FDA 510(k) Applications Submitted by DOMINIQUE GRENIER

FDA 510(k) Number Submission Date Device Name Applicant
K040753 03/24/2004 R-TEST EVOLUTION 3 NOVACOR
K042108 08/04/2004 VISTA PLUS NOVACOR
K042109 08/05/2004 DIASYS INTEGRA II NOVACOR FRANCE


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